PMC:7534795 / 52133-52363 JSONTXT

{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T219","span":{"begin":102,"end":106},"obj":"Body_part"}],"attributes":[{"id":"A219","pred":"fma_id","subj":"T219","obj":"http://purl.org/sig/ont/fma/fma256135"}],"text":"y and non-dietary sources. The simplest n-3 PUFA is α-linolenic acid (ALA, 18:3 n-3). Once inside the body, ALA can be converted through a series of elongation and desaturation reactions into other n-3 PUFAs. For instance, ALA is "}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T313","span":{"begin":75,"end":77},"obj":"http://purl.obolibrary.org/obo/CLO_0050510"},{"id":"T314","span":{"begin":137,"end":138},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"}],"text":"y and non-dietary sources. The simplest n-3 PUFA is α-linolenic acid (ALA, 18:3 n-3). Once inside the body, ALA can be converted through a series of elongation and desaturation reactions into other n-3 PUFAs. For instance, ALA is "}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T1123","span":{"begin":44,"end":48},"obj":"Chemical"},{"id":"T18159","span":{"begin":54,"end":68},"obj":"Chemical"},{"id":"T92595","span":{"begin":64,"end":68},"obj":"Chemical"},{"id":"T6817","span":{"begin":70,"end":73},"obj":"Chemical"},{"id":"T65","span":{"begin":75,"end":79},"obj":"Chemical"},{"id":"T46099","span":{"begin":108,"end":111},"obj":"Chemical"},{"id":"T15635","span":{"begin":202,"end":207},"obj":"Chemical"},{"id":"T68740","span":{"begin":223,"end":226},"obj":"Chemical"}],"attributes":[{"id":"A29348","pred":"chebi_id","subj":"T1123","obj":"http://purl.obolibrary.org/obo/CHEBI_26208"},{"id":"A98566","pred":"chebi_id","subj":"T1123","obj":"http://purl.obolibrary.org/obo/CHEBI_76567"},{"id":"A95245","pred":"chebi_id","subj":"T18159","obj":"http://purl.obolibrary.org/obo/CHEBI_25048"},{"id":"A30449","pred":"chebi_id","subj":"T18159","obj":"http://purl.obolibrary.org/obo/CHEBI_27432"},{"id":"A47485","pred":"chebi_id","subj":"T92595","obj":"http://purl.obolibrary.org/obo/CHEBI_37527"},{"id":"A61272","pred":"chebi_id","subj":"T6817","obj":"http://purl.obolibrary.org/obo/CHEBI_16449"},{"id":"A8915","pred":"chebi_id","subj":"T6817","obj":"http://purl.obolibrary.org/obo/CHEBI_27432"},{"id":"A31130","pred":"chebi_id","subj":"T65","obj":"http://purl.obolibrary.org/obo/CHEBI_25633"},{"id":"A73275","pred":"chebi_id","subj":"T65","obj":"http://purl.obolibrary.org/obo/CHEBI_61160"},{"id":"A5753","pred":"chebi_id","subj":"T46099","obj":"http://purl.obolibrary.org/obo/CHEBI_16449"},{"id":"A28600","pred":"chebi_id","subj":"T46099","obj":"http://purl.obolibrary.org/obo/CHEBI_27432"},{"id":"A68057","pred":"chebi_id","subj":"T15635","obj":"http://purl.obolibrary.org/obo/CHEBI_26208"},{"id":"A37582","pred":"chebi_id","subj":"T68740","obj":"http://purl.obolibrary.org/obo/CHEBI_16449"},{"id":"A80563","pred":"chebi_id","subj":"T68740","obj":"http://purl.obolibrary.org/obo/CHEBI_27432"}],"text":"y and non-dietary sources. The simplest n-3 PUFA is α-linolenic acid (ALA, 18:3 n-3). Once inside the body, ALA can be converted through a series of elongation and desaturation reactions into other n-3 PUFAs. For instance, ALA is "}

{"project":"LitCovid-sentences","denotations":[{"id":"T427","span":{"begin":27,"end":85},"obj":"Sentence"},{"id":"T428","span":{"begin":86,"end":208},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"y and non-dietary sources. The simplest n-3 PUFA is α-linolenic acid (ALA, 18:3 n-3). Once inside the body, ALA can be converted through a series of elongation and desaturation reactions into other n-3 PUFAs. For instance, ALA is "}

{"project":"LitCovid-PubTator","denotations":[{"id":"1564","span":{"begin":44,"end":48},"obj":"Gene"},{"id":"1570","span":{"begin":52,"end":68},"obj":"Chemical"},{"id":"1571","span":{"begin":70,"end":73},"obj":"Chemical"},{"id":"1572","span":{"begin":108,"end":111},"obj":"Chemical"},{"id":"1573","span":{"begin":198,"end":207},"obj":"Chemical"},{"id":"1574","span":{"begin":223,"end":226},"obj":"Chemical"}],"attributes":[{"id":"A1564","pred":"tao:has_database_id","subj":"1564","obj":"Gene:9933"},{"id":"A1570","pred":"tao:has_database_id","subj":"1570","obj":"MESH:D017962"},{"id":"A1571","pred":"tao:has_database_id","subj":"1571","obj":"MESH:D017962"},{"id":"A1572","pred":"tao:has_database_id","subj":"1572","obj":"MESH:D017962"},{"id":"A1573","pred":"tao:has_database_id","subj":"1573","obj":"MESH:D015525"},{"id":"A1574","pred":"tao:has_database_id","subj":"1574","obj":"MESH:D017962"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"y and non-dietary sources. The simplest n-3 PUFA is α-linolenic acid (ALA, 18:3 n-3). Once inside the body, ALA can be converted through a series of elongation and desaturation reactions into other n-3 PUFAs. For instance, ALA is "}